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• 42444-51-9 3,5-dinitrobenzoyl azide 
• 130857-42-0 (1S,3R,5aS,7aS,7bR)-1-hydroxy-7b-methyl-2-oxo-5a,6,7,7a-tetrahydrocyclopenta-<1,2,3-gi>pyrrolidino<1,2-a>pyrrolidine 
• 124126-12-1 rel-(1R,3S,5aR,7aR,7bS)-1-hydroxy-7b-methyl-2-oxo-5a,6,7,7a-tetrahydrocyclopenta<1,2,3-gi>pyrrolidino<1,2-a>pyrrolidine 

Relevant academic research and scientific papers

Tandem Inter /Intra Nitroalkene Cycloadditions. 5. Origin of the Lewis Acid Dependent Reversal of Stereoselektivity

The stereochemical course of the tandem / nitroalkene cycloaddition with chiral enol ethers has been shown to exhibit remarkable sensitivity to the nature of the Lewis acid promoter.Cycloadditions using (+)-camphor-derived vinyl ether 3 or (-)-t

TANDEM /-CYCLOADDITIONS. 2. ASYMMETRIC INDUCTION WITH A CHIRAL VINYL ETHER

A tandem /-cycloaddition of nitroalkenes tethered to α,Sb-unsaturated ester dipolarophiles can be effectively triggered with a vinyl ether.Using the chiral vinyl ether 6 as the dienophile, nitroalkenes 1 and 2 undergo highly selective tandem cyc